Differentiating Benign from Malignant Causes of Splenomegaly: Is Acoustic Radiation Force Impulse Elastography Helpful?

被引:0
作者
Alhyari, Amjad [1 ,2 ]
Dob, Oussama [3 ]
Safai Zadeh, Ehsan [4 ]
Dietrich, Christoph Frank [5 ]
Trenker, Corrina [2 ,6 ]
Gress, Thomas M. [1 ]
Goerg, Christian [1 ,2 ]
机构
[1] Philipp Univ Marburg, Univ Hosp Giessen & Marburg, Gastroenterol Endocrinol Metab & Clin Infectiol, Baldingerstr, D-35037 Marburg, Germany
[2] Philipp Univ Marburg, Univ Hosp Giessen & Marburg, Interdisciplinary Ctr Ultrasound Diagnost, Baldingerstr, D-35037 Marburg, Germany
[3] Philipp Univ Marburg, Univ Hosp Giessen & Marburg, Dept Radiol, D-35037 Marburg, Germany
[4] Med Univ Vienna, Dept Biomed Imaging & Image Guided Therapy, A-1019 Vienna, Austria
[5] Kliniken Hirslanden Bern, Dept Allgemeine Innere Med DAIM, Beau Site, CH-3013 Bern, Switzerland
[6] Philipps Univ Marburg, Univ Hosp Giessen & Marburg, Hematol Oncol & Immunol, Baldingerstr, D-35037 Marburg, Germany
关键词
ARFI; spleen; point shear wave elastography; ultrasound; splenomegaly; SPLEEN STIFFNESS MEASUREMENTS; SHEAR-WAVE ELASTOGRAPHY; ULTRASOUND ELASTOGRAPHY; LIVER;
D O I
10.3390/diseases12120308
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: To evaluate the ability of acoustic radiation force impulse (ARFI) elastography in differentiating benign from malignant etiologies of splenomegaly based on differences in splenic stiffness. Materials and Methods: Between September 2020 and November 2022, we evaluated 40 patients with splenomegaly-defined by a splenic long axis greater than 13 cm and/or a short axis greater than 6 cm, without visible focal or infiltrative mass lesions-using abdominal ultrasound at our university hospital. Each patient also underwent a standardized ARFI elastographic assessment of the enlarged spleen, with data collected prospectively. We then retrospectively analyzed the cases with confirmed etiologies of splenomegaly from their final medical reports. Mean ARFI velocities (MAV) were compared across patients with splenomegaly due to malignant infiltration (MIS) from hematological malignancy, congestive splenomegaly (CS) due to portal or splenic vein congestion/occlusion, and immune-related splenomegaly (IRS) associated with systemic infectious or autoimmune diseases. Results: Among the 40 patients with splenomegaly, 21 (52.5%) were diagnosed with malignant infiltrative splenomegaly (MIS), 11 (27.5%) with congestive splenomegaly (CS), and 8 (20%) with immune-related splenomegaly (IRS). The mean ARFI velocities (MAV) for the MIS, CS, and IRS groups were 3.25 +/- 0.68 m/s, 3.52 +/- 0.47 m/s, and 2.84 +/- 0.92 m/s, respectively. No significant differences were observed in splenic stiffness (MAV) among these groups. Conclusions: Differentiating between benign and malignant etiologies of splenomegaly based on stiffness differences observed in ARFI elastography is not feasible. Larger prospective studies are necessary to validate these findings.
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